Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,993 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,993 in last 12 months

Showing 1242112440 of 56,506 recalls

DrugAugust 10, 2022· Nephron Sc Inc

Recalled Item: Ketorolac Tromethamine Injection Recalled by Nephron Sc Inc Due to cGMP...

The Issue: cGMP Deviations: deviations leading to potential cross-contamination.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-0.125% Bupivacaine HCl Injection Recalled by Nephron Sterile Compounding...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Trisodium Citrate 0.5% Solution Recalled by Nephron Sterile Compounding...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2022· Angiodynamics, Inc.

Recalled Item: VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog Recalled by...

The Issue: OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Steris Corporation Hopkins Facility

Recalled Item: Verify SixCess Challenge Pack. Used to confirm that critical parameters...

The Issue: Product contains incorrect chemical indicators in packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceAugust 10, 2022· Saranas, Inc.

Recalled Item: Early Bird Bleed Monitoring System Introducer Sheath Set Recalled by...

The Issue: Bleed monitoring system device design error, causing the device to not power...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· DEWEI MEDICAL EQUIPMENT CO LTD

Recalled Item: Dewei DNA/RNA Preservation Kit Recalled by DEWEI MEDICAL EQUIPMENT CO LTD...

The Issue: Products were distributed in the United States without FDA authorization or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2022· Jiangsu Well Biotech Co.,Ltd.

Recalled Item: Jiangsu Well Biotech Co. Recalled by Jiangsu Well Biotech Co.,Ltd. Due to...

The Issue: Distribution of COVID-19 Ag Rapid Test kits in the U.S. without an Emergency...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2022· Hologic, Inc

Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...

The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...

The Issue: Firm noted an increase in customer reports of leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2022· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: Burns of varying degrees can occur to patients with electrodes left in while...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 8, 2022· Akorn, Inc

Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...

The Issue: Identification of an unknown impurity at the 12-month stability point....

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 8, 2022· GS Biomark LLC

Recalled Item: CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200...

The Issue: Distribution of COVID Test Kits without FDA Approval, Clearance or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 4, 2022· LNK International, Inc.

Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...

The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2022· That's it. Nutrition, LCC

Recalled Item: That's It. Dark Chocolate Raisin Truffles Net WT. 3.5 oz Recalled by That's...

The Issue: CFIA testing of the products revealed casein and whey which caused...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2022· That's it. Nutrition, LCC

Recalled Item: That's It. Dark Chocolate Fig with Sea Salt Truffles Net WT. 3.5 oz Recalled...

The Issue: CFIA testing of the products revealed casein and whey which caused...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund